EMMA™ is designed to support clinician‑reviewed documentation, analytics, and post‑procedure review workflows. It does not provide autonomous clinical decision‑making, intra‑procedural guidance, or therapeutic recommendations.
All outputs generated by EMMA™ are intended for clinician review. The platform is designed to augment clinical workflows, not replace professional judgment.
VisionMed follows a validation‑first approach to platform development, emphasizing measurable performance, auditability, and consistency across clinical environments.
The EMMA™ platform is not intended for diagnostic, therapeutic, or clinical decision-making purposes. It does not perform diagnostic interpretation of medical data, make treatment recommendations, or function as a medical device under FDA definitions. EMMA provides draft clinical documentation for healthcare provider review only. All clinical decisions remain solely in the hands of licensed medical professionals.
VisionMed prioritizes data security, privacy, and controlled data handling. Deployment models support enterprise governance requirements without vendor lock‑in.
Partner with VisionMed to advance procedural documentation, insight, and intelligence. Contact us to learn more, explore collaborations, or request a live demo.
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